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pro vyhledávání: '"Douglas B. Webster"'
Autor:
Douglas B. Webster
Publikováno v:
Evolution, Brain, and Behavior: Persistent Problems ISBN: 9781315787107
Evolution, Brain, and Behavior: Persistent Problems
Evolution, Brain, and Behavior: Persistent Problems
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d85d05a441702d4b4d9755d539456420
https://doi.org/10.4324/9781315787107-1
https://doi.org/10.4324/9781315787107-1
Autor:
Douglas B Webster, Richard R. Fay
The Springer Handbook of Auditory Research presents a series of com prehensive and synthetic reviews of the fundamental topics in modem auditory research. It is aimed at all individuals with interests in hearing research including advanced graduate
Publikováno v:
Hearing Research. 133:27-39
Thirty-six drug deafened guinea pigs were studied to determine how electrical stimulation of the cochlea affects spiral ganglion cell (SGC) survival. Animals were divided into two groups, extracochlear and intracochlear stimulation, and each group wa
Autor:
Douglas B. Webster, Richard R. Fay
To develop a science of hearing that is intellectu The five-day conference was held at the Mote ally satisfying we must first integrate the diverse, Marine Laboratory in Sarasota, Florida, May - extensive body of comparative research into an 24, 19
Autor:
Michael E. Walsh, Douglas B. Webster
Publikováno v:
Hearing Research. 75:54-60
Both CBA/J mice with neonatal cochlea removals and CBA/J mice with neonatal atresias of the external auditory meatus have significantly smaller ventral cochlear nucleus is greater in the mice with cochlea removals, but the soma area reduction is grea
Publikováno v:
Hearing Research. 67:51-54
Cochlear degeneration in the early postnatal period has been reported as a homozygous recessive mutation in deafness (dn/dn) mice of the curly-tail stock. Heterozygous (+ /dn) mice of the same population exhibit hearing when tested by the Preyer refl
Autor:
Douglas B. Webster
Publikováno v:
Experimental Neurology. 115:27-31
The deafness mouse is a Mendelian recessive mutant which never hears and has no stimulus-related receptor or neural auditory responses. From birth through 12 days after birth (DAB), the organ of Corti develops normally as seen with light microscopy,
Autor:
Charles I. Berlin, Jer-Min Huang, Douglas B. Webster, N. Nouri, Bronya J.B. Keats, Matthew K. Money
Publikováno v:
Mammalian Genome. 6:8-10
The deafness mouse has profound sensorineural hearing loss with degeneration of hair cells soon after birth. The mode of inheritance is recessive, and there are no associated phenotypic anomalies. Thus, this mouse provides a model for recessive, non-
Autor:
Jer-Min Huang, Chen Xie, Phil Skolnick, Douglas B. Webster, Anthony S. Basile, Charles I. Berlin
Publikováno v:
Nature medicine. 2(12)
The use of aminoglycoside antibiotics is limited by ototoxicity that can produce permanent hearing loss. We report that concurrent administration of N-methyl-D-aspartate (NMDA) antagonists markedly attenuates both the hearing loss and destruction of
Publikováno v:
Hearing research. 87(1-2)
Exogenous administration of GM1 ganglioside to CBA/J mice with a neonatal conductive hearing loss ameliorates the atrophy of spiral ganglion neurons, ventral cochlear nucleus neurons, and ventral cochlear nucleus volume. The present investigation dem